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Active substance: ECHINACEA ANGUSTIFOLIA, PHYTOLACCA AMERICANA ROOT, SUS SCROFA LYMPH, CONIUM MACULATUM FLOWERING TOP, FERROUS IODIDE, CALCIUM SULFIDE, POTASSIUM CHLORIDE, LACHESIS MUTA VENOM, SILICON DIOXIDE
LIQUID · ECHINACEA ANGUSTIFOLIA 3 [hp_X]/mL, PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL, SUS SCROFA LYMPH 6 [hp_X]/mL, CONIUM MACULATUM FLOWERING TOP 12 [hp_X]/mL, FERROUS IODIDE 12 [hp_X]/mL, CALCIUM SULFIDE 12 [hp_X]/mL, POTASSIUM CHLORIDE 12 [hp_X]/mL, LACHESIS MUTA VENOM 12 [hp_X]/mL, SILICON DIOXIDE 12 [hp_X]/mL
United StatesActive
Marketing holder: Supplement Clinic, LLC.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
Composition
- ECHINACEA ANGUSTIFOLIA · 3 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT · 3 [hp_X]/mL
- SUS SCROFA LYMPH · 6 [hp_X]/mL
- CONIUM MACULATUM FLOWERING TOP · 12 [hp_X]/mL
- FERROUS IODIDE · 12 [hp_X]/mL
- CALCIUM SULFIDE · 12 [hp_X]/mL
- POTASSIUM CHLORIDE · 12 [hp_X]/mL
- LACHESIS MUTA VENOM · 12 [hp_X]/mL
- SILICON DIOXIDE · 12 [hp_X]/mL
Registration
- Registration number
- 71781-0004
- Registration status
- Active
- Dispensing
- Over the counter
- Route
- ORAL
Sources
- product · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.4 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.5 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.6 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.7 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source
- ingredients.8 · openFDA NDC · 71781-0004 · Verified 2026-10-09 · open in source